Fusion Gene Studies
in Kim Lab

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Center for Computational Systems Medicine
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Fusion Gene Summary

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Fusion Gene ORF analysis

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Fusion Genomic Features

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Fusion Protein Features

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Fusion Gene Sequence

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Fusion Gene PPI analysis

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Related Drugs

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Related Diseases

Fusion gene:ATP5I-CBX5 (FusionGDB2 ID:HG521TG23468)

Fusion Gene Summary for ATP5I-CBX5

check button Fusion gene summary
Fusion gene informationFusion gene name: ATP5I-CBX5
Fusion gene ID: hg521tg23468
HgeneTgene
Gene symbol

ATP5I

CBX5

Gene ID

521

23468

Gene nameATP synthase membrane subunit echromobox 5
SynonymsATP5I|ATP5KHEL25|HP1|HP1A
Cytomap('ATP5I')('CBX5')

4p16.3

12q13.13

Type of geneprotein-codingprotein-coding
DescriptionATP synthase subunit e, mitochondrialATP synthase e chain, mitochondrialATP synthase, H+ transporting, mitochondrial F0 complex, subunit EATP synthase, H+ transporting, mitochondrial Fo complex subunit EATPase subunit eF1F0-ATP synthase, murine e subchromobox protein homolog 5HP1 alpha homologHP1-ALPHAHP1Hs alphaantigen p25chromobox homolog 5 (HP1 alpha homolog, Drosophila)epididymis luminal protein 25heterochromatin protein 1 homolog alphaheterochromatin protein 1-alpha
Modification date2020031320200313
UniProtAcc..
Ensembl transtripts involved in fusion geneENST00000506525, ENST00000304312, 
Fusion gene scores* DoF score9 X 9 X 4=3249 X 9 X 4=324
# samples 129
** MAII scorelog2(12/324*10)=-1.43295940727611
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(9/324*10)=-1.84799690655495
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: ATP5I [Title/Abstract] AND CBX5 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointATP5I(667092)-CBX5(54635689), # samples:1
Anticipated loss of major functional domain due to fusion event.ATP5I-CBX5 seems lost the major protein functional domain in Hgene partner, which is a CGC by not retaining the major functional domain in the partially deleted in-frame ORF.
ATP5I-CBX5 seems lost the major protein functional domain in Hgene partner, which is a essential gene by not retaining the major functional domain in the partially deleted in-frame ORF.
ATP5I-CBX5 seems lost the major protein functional domain in Hgene partner, which is a essential gene due to the frame-shifted ORF.
ATP5I-CBX5 seems lost the major protein functional domain in Tgene partner, which is a epigenetic factor due to the frame-shifted ORF.
ATP5I-CBX5 seems lost the major protein functional domain in Tgene partner, which is a essential gene due to the frame-shifted ORF.
ATP5I-CBX5 seems lost the major protein functional domain in Tgene partner, which is a tumor suppressor due to the frame-shifted ORF.
* DoF score (Degree of Frequency) = # partners X # break points X # cancer types
** MAII score (Major Active Isofusion Index) = log2(# samples/DoF score*10)

check button Gene ontology of each fusion partner gene with evidence of Inferred from Direct Assay (IDA) from Entrez
PartnerGeneGO IDGO termPubMed ID
HgeneATP5I

GO:0042776

mitochondrial ATP synthesis coupled proton transport

12110673

TgeneCBX5

GO:0045892

negative regulation of transcription, DNA-templated

9636147


check buttonFusion gene breakpoints across ATP5I (5'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.
all structure
check buttonFusion gene breakpoints across CBX5 (3'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.
all structure

check button Fusion gene information
* All genome coordinats were lifted-over on hg19.
* Click on the break point to see the gene structure around the break point region using the UCSC Genome Browser.
SourceDiseaseSampleHgeneHchrHbpHstrandTgeneTchrTbpTstrand
ChimerDB4GBMTCGA-27-2519-01AATP5Ichr4

667092

-CBX5chr12

54635689

-


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Fusion Gene ORF analysis for ATP5I-CBX5

check button Open reading frame (ORF) analsis of fusion genes based on Ensembl gene isoform structure.
* Click on the break point to see the gene structure around the break point region using the UCSC Genome Browser.
ORFHenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrand
5UTR-3CDSENST00000506525ENST00000209875ATP5Ichr4

667092

-CBX5chr12

54635689

-
5UTR-3CDSENST00000506525ENST00000439541ATP5Ichr4

667092

-CBX5chr12

54635689

-
5UTR-3CDSENST00000506525ENST00000550411ATP5Ichr4

667092

-CBX5chr12

54635689

-
Frame-shiftENST00000304312ENST00000439541ATP5Ichr4

667092

-CBX5chr12

54635689

-
Frame-shiftENST00000304312ENST00000550411ATP5Ichr4

667092

-CBX5chr12

54635689

-
In-frameENST00000304312ENST00000209875ATP5Ichr4

667092

-CBX5chr12

54635689

-

check buttonORFfinder result based on the fusion transcript sequence of in-frame fusion genes.
HenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrandSeq length
(transcript)
BP loci
(transcript)
Predicted start
(transcript)
Predicted stop
(transcript)
Seq length
(amino acids)
ENST00000304312ATP5Ichr4667092-ENST00000209875CBX5chr1254635689-112472811044610919157

check buttonDeepORF prediction of the coding potential based on the fusion transcript sequence of in-frame fusion genes. DeepORF is a coding potential classifier based on convolutional neural network by comparing the real Ribo-seq data. If the no-coding score < 0.5 and coding score > 0.5, then the in-frame fusion transcript is predicted as being likely translated.
HenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrandNo-coding scoreCoding score
ENST00000304312ENST00000209875ATP5Ichr4667092-CBX5chr1254635689-0.53746550.46253452

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Fusion Genomic Features for ATP5I-CBX5


check buttonFusionAI prediction of the potential fusion gene breakpoint based on the pre-mature RNA sequence context (+/- 5kb of individual partner genes, total 20kb length sequence). FusionAI is a fusion gene breakpoint classifier based on convolutional neural network by comparing the fusion positive and negative sequence context of ~ 20K fusion gene data. From here, we can have the relative potentency of the 20K genomic sequence how individual sequnce will be likely used as the gene fusion breakpoints.
HgeneHchrHbpHstrandTgeneTchrTbpTstrand1-pp (fusion gene breakpoint)

check buttonDistribution of 44 human genomic features loci across 20kb length fusion breakpoint regions. We integrated a total of 44 different types of human genomic feature loci information across five big categories including virus integration sites, repeats, structural variants, chromatin states, and gene expression regulation. More details are in help page.
genomic feature

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Fusion Protein Features for ATP5I-CBX5


check button Four levels of functional features of fusion genes
Go to FGviewer search page for the most frequent breakpoint (https://ccsmweb.uth.edu/FGviewer/chr4:667092/chr12:54635689)
- FGviewer provides the online visualization of the retention search of the protein functional features across DNA, RNA, protein, and pathological levels.
- How to search
1. Put your fusion gene symbol.
2. Press the tab key until there will be shown the breakpoint information filled.
4. Go down and press 'Search' tab twice.
4. Go down to have the hyperlink of the search result.
5. Click the hyperlink.
6. See the FGviewer result for your fusion gene.
FGviewer

check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
..
FUNCTION: Transcriptional activator which is required for calcium-dependent dendritic growth and branching in cortical neurons. Recruits CREB-binding protein (CREBBP) to nuclear bodies. Component of the CREST-BRG1 complex, a multiprotein complex that regulates promoter activation by orchestrating a calcium-dependent release of a repressor complex and a recruitment of an activator complex. In resting neurons, transcription of the c-FOS promoter is inhibited by BRG1-dependent recruitment of a phospho-RB1-HDAC1 repressor complex. Upon calcium influx, RB1 is dephosphorylated by calcineurin, which leads to release of the repressor complex. At the same time, there is increased recruitment of CREBBP to the promoter by a CREST-dependent mechanism, which leads to transcriptional activation. The CREST-BRG1 complex also binds to the NR2B promoter, and activity-dependent induction of NR2B expression involves a release of HDAC1 and recruitment of CREBBP (By similarity). {ECO:0000250}.FUNCTION: Transcriptional activator which is required for calcium-dependent dendritic growth and branching in cortical neurons. Recruits CREB-binding protein (CREBBP) to nuclear bodies. Component of the CREST-BRG1 complex, a multiprotein complex that regulates promoter activation by orchestrating a calcium-dependent release of a repressor complex and a recruitment of an activator complex. In resting neurons, transcription of the c-FOS promoter is inhibited by BRG1-dependent recruitment of a phospho-RB1-HDAC1 repressor complex. Upon calcium influx, RB1 is dephosphorylated by calcineurin, which leads to release of the repressor complex. At the same time, there is increased recruitment of CREBBP to the promoter by a CREST-dependent mechanism, which leads to transcriptional activation. The CREST-BRG1 complex also binds to the NR2B promoter, and activity-dependent induction of NR2B expression involves a release of HDAC1 and recruitment of CREBBP (By similarity). {ECO:0000250}.

check buttonRetention analysis result of each fusion partner protein across 39 protein features of UniProt such as six molecule processing features, 13 region features, four site features, six amino acid modification features, two natural variation features, five experimental info features, and 3 secondary structure features. Here, because of limited space for viewing, we only show the protein feature retention information belong to the 13 regional features. All retention annotation result can be downloaded at

download page


* Minus value of BPloci means that the break pointn is located before the CDS.
- In-frame and retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note

- In-frame and not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
TgeneCBX5chr4:667092chr12:54635689ENST000002098753511_14141192.0Compositional biasNote=Poly-Ser
TgeneCBX5chr4:667092chr12:54635689ENST000004395413511_14141192.0Compositional biasNote=Poly-Ser
TgeneCBX5chr4:667092chr12:54635689ENST000005504113511_14141192.0Compositional biasNote=Poly-Ser
TgeneCBX5chr4:667092chr12:54635689ENST0000020987535121_179141192.0DomainChromo 2%3B shadow subtype
TgeneCBX5chr4:667092chr12:54635689ENST000002098753520_78141192.0DomainChromo 1
TgeneCBX5chr4:667092chr12:54635689ENST0000043954135121_179141192.0DomainChromo 2%3B shadow subtype
TgeneCBX5chr4:667092chr12:54635689ENST000004395413520_78141192.0DomainChromo 1
TgeneCBX5chr4:667092chr12:54635689ENST0000055041135121_179141192.0DomainChromo 2%3B shadow subtype
TgeneCBX5chr4:667092chr12:54635689ENST000005504113520_78141192.0DomainChromo 1


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Fusion Gene Sequence for ATP5I-CBX5


check button For in-frame fusion transcripts, we provide the fusion transcript sequences and fusion amino acid sequences. To have fusion amino acid sequence, we ran ORFfinder and chose the longest ORF among the all predicted ones.
>7995_7995_1_ATP5I-CBX5_ATP5I_chr4_667092_ENST00000304312_CBX5_chr12_54635689_ENST00000209875_length(transcript)=11247nt_BP=281nt
AGCTCCGCCTTTGCCTCCAAGGCTTTGCTGGCTTGTGCGGCATCCTGCTCCGTCTGCAGGTTGTGCTTCCGGTGCGGAGGTCAGGGACAA
GATGGTGCCACCGGTGCAGGTCTCTCCGCTCATCAAGCTCGGCCGCTACTCCGCCCTGTTCCTCGGTGTGGCCTACGGAGCCACGCGCTA
CAATTACCTAAAACCTCGGGCAGAAGAGGAGAGGAGGATAGCAGCAGAAGAGAAGAAGAAGCAGGATGAACTGAAACGGATTGCCAGAGA
ATTGGCAGAAGGAAAGACACAGATGAAGCTGACCTGGTTCTTGCAAAAGAAGCTAATGTGAAATGTCCACAAATTGTGATAGCATTTTAT
GAAGAGAGACTGACATGGCATGCATATCCTGAGGATGCGGAAAACAAAGAGAAAGAAACAGCAAAGAGCTAAAGGAGGGGATGGTCTCTG
TCATTTCTCTTTGTACATAATACATTCACCTCCCTGCCTCCTCTCCTTTCTACCCACCCCTTTCTATCCTAAACACATCCATAAAAAATG
TGCTTATCACTGTGCTCCACAGGAGAAATGTTGGTATTGGTTCTCTTGTAACATAACTGATGGTCTGATTAATGATAAGTGTCTCTCTGT
GAAGACCAGGCATTTACATACTGAGTGTAATACCCACAATTTTTTTTTCCTTTGCCCTGATCTCTTCCTTCTGCTTCCCTGTGACCTCAA
GATGAGTTTCAACTTTTTAATCACCTTAGAGTCTTGATCTTTTCAGGGTTGGTCGCTTTTTAGGTTGGGGGATTTTGTTACAATGATGTT
GAATTTTGGTTTCTTGCTTTGGTTCTTAGAACATGTTGCTGACTAGCTGGCCTTTGTTCTGACATGTTGAGATGGAAAGGATGTTGCCCA
TCTGTTAAAAAGCCAATAGCAACTGCCTACCTGTTGGGGCTTTCCCAACCTTGTTCAGCTCTACCCAGGAGAATACAGGGTTTCTGGTGT
GGTCTTCTGGGCCACCCTCTGTTGTTCATCCTCACTCATCCTCCCAGAATTACTCCATCCTTTGGAAGATTTGAAATTTTACACTGAAAT
CTGTCAAGACACTCTTTTTAGCCCCAGGACTTTCGGTATTGCTTTTAGCACTCCCCACTTCTGCTTCTGTAAAGTGATATCAATTTGTGA
TAAAATGACAAGATTATTAACTGTGCAGATTTGTAGCTATAGTACATGAGGATGATGGGGTAGGGTACAATTGTCTTTATTATCATATAT
GGTATGTATGTATGATTTCTTTCCATTCCTCATATTTAGACTGTATATTTATGTAGGTGTGAGTGATTGCCTGGTGCTTGCTTGTGCCAA
GGTGCTAGGCACCCTCCAACCCTGCCAACTTTTGTGGCCTCCCAAAGCATTCCTGTTACCAAAGAGGCTTCAAACCTGACCCTCACTTCT
CAGTGGACCCGAGTTTCCCTTCCATGCCATTATTTTCAGTGGGGAAGTTTTAGAGGTGAGCTGTTGGCCACAATATCAATTTTAAGTGTT
CATAGCAGTTATGTCTCCTGCATTCTTGGCTCCTGGATTTACCACCAAGAGTCCCCAAAATATTAATGCTCTTCCCTTTTTCTACCCTCA
AACTTATAGTTGTATCTTATTTTTTAAAATGAATTTTCATGGCCAGGCACAGTGGCTACCGCCTGTAATCCCAGCACTTTGGGAGGCTGA
GGCAGGAGAATTGCTTGAAGCCAGAAGTTTGAGACCAGCCTGGGCAATGTAGTGAGACCCCCTGTCTCTAAAAAATATAAATAAAAATAA
AGGCATGTTCCTGAAAGACTGTCACCTTGGAAAGTGACAGGCCCTGGCATTAGCATGTTGACACACCCTTTTCTTCTTACTCAGCAAAAT
ACTTCGTTTTGGTTTCTTCTTGTGTTGCTATTGAGAAATTTGTCTGATCATATCCTTCTGCCTTTGTCCCCCAAGAAATGCCCTACTTTA
TCCTTTTCTTTTTGTAGTTGAGGAGGGCTAGAGAATCACAATTAAAAGTAAGGAAATAGCAGGGTTTTGAGGATCCTTGTCCCAGCCCCA
AAGCTGAGGAAATAAGAATAAATGCTTAATATAGCCTTAATTCTAGAGCGCACCAGCCATGAGGCTGCTTTTCTTGTTGTTTTTGATTTT
TAAAACATACAGCTGTCTGGCCAGGAGCATCTACCATTTCTAGATTATTCAGAGTAATGAGGGGAATGGATGGATTGCTCCAGTCCACAG
ATGAGCCACATAATATGCAAATCATATACCCATTCATAGCATTTGTTAACATTGCTTCCCTGCTCAGCTGCTGATTGAATTCTGTGTGCT
TATATAAATTATGTCAAAAATTATACTGCATAATTGAGGTGACAGCTGTTGCTGCAGTGACATGACAGACTGGAACAATGAAGCTTTTGG
TTTAAGTCAGCCAGGAAAATCCTTCTGAATGGTAATGTGATTGGGCAAGAGCTCATAAACCATACCTCAAGTGGGTGGGAGTTTTATCTC
TATATTCCTTCTCTCTCTGAAGGAATTAAAGGCCTAGATCAAGTGCTGGATAATTGACAATTGCTTGTACTTAATCTGATCGGTATCTAA
AAGAAGGAAAGGATGGTCAGGAAACATTTATCATAAATGTAGCCAAGGATATCAATTAGGGTAGACAAGAATAGGACAAAAATAGGCCAG
AGCTCCTGAGGAGGTGATATGGGTCTCTTGATTTGCAGAAAATGACAGCCTATCCAAGTGGCCCAGTGTATGCCTCCCAGTAGCAGTGGG
CATGTAAACTGCAGCGACCTTATTTTTAAAACCAAAAACCTAGTATGTGGACAAAGAACATGACAATATTTGGTACTGAGATTGGTTCTG
AGAAACCTGGGGCATGTGGCTGCTGTGGTTATAGGTAATATTTAAGACATTCATAAAAATCTGATATTCTTTTACCGAAATAACCCCAGT
ATCATCTACTACTTACCATCTGTTAATAGACTTTACTCTGTCTTTTTTGTCTTCGGTTTATTGTACTGAGTGCCGCCAAAACAACTTTTG
TTCTCTTCCTGCCTACCTGCAGCTGGTTCTATAGGAATGTAGGGAGCCAGAGGCCAGTATTGATTTCAGCCCTTAGCACAAAGGAAATCA
GATGCCTGCTTCCAGCATTTGTTAGTGTTGAGTAGATGTTCTTGCCCTAGAAGAATTACAGCCTCAAACAGAAACCTGTTTCATGGAGCT
TTCTCCCCTCAGAAGAGTTAATAGTTAAGAGCTAAGCACTCTTAAACACCTAAGTCTCAAATGCTAAAAATTTATTTTTCTTGTGTTTAG
TCCTCTTTCAAGACATCTTTCTAAGCCTTTCAGTAATCAACATTAAAAGATCTCCCTTTCTTCAGAGTTATAGCACAGCTTTGCCCAGTA
GAGGCTACCAAGGACAGCTTAGCAGCCCTTTGATTGCTGGGCTGGGCAGATGGCCTTCAAGTTAAGATCAAATGCCGGGAAAATCAGCCT
ACATGGGAGCACCCATTTTAAACCTGGAGAGAACCATGATGTTTTCTTCTTCAAATAACAATCTAGTTTTTTTTCCCCCAGTACTAAAAT
TGTATTGTCTTTCAGACAATATAATTTTTATTTAAAATTGGAACATACTATCTTCATGCTTTCTAAGCTAAATCTTCATTTAGATTTCAC
TCCTCAGTAGATCCCAGAGAAGAAGCTATATAGGATCCAGATTCAAATTTAACAGTGTCTTCTACTTTTTTAGTTATGTTTTCTATCAAC
TCCTGCTGCCTTTTCAAATACGGATATTTTTCAGGAGACTCTTCTACTTGTCCACTGACTGTATTTTTTCCTTTTTGATCCGTAGCCCTG
GTTAAATGGCTGACATCCTTCCGTGGATGATTCTTGGAGGTAGTCTCAGAATTCCAAAGTGATTGTCTGTCTTCTTCTTGTCTTGATCCT
AATGCAGACATTCACCTCTATTATTTATTTATTTTTTTTAGACAGAGTCTCGCTCTGTCACCAGGCTGGAGTGCAGTGGCACAATCTTGG
CTTACTGTACCCTCCACCTCCTGGGTTCAAGCGATTCTCCTGCCTCAGCCTCTCGAGTAGCTGGGACTACAGGTGTGTGCCACCATGCCC
AGCTAATTTTTGTATTTTTGGTAGAGATGGGGTTTTACCATGTTTGCCAGGATGGTCTCGATTTCCTGACCTTGTGATCTGCCCACCTTG
GCCTCCCAAAGTGCTGGAATTACAGGCATGAGCCACCGTGCCTGGCCACCTCTATTAAATTTTTGTGGACAAAAATAAAATTGTCATTAT
TTGTTTGCTCTCATGGAGCACTTTCAGTAATACAATTTTTTTTAAATTCCAGTTGCCCTCTTTGTTGCTCTGTCCTCTGTAATACCTGAC
TTTGCTAAAGACTTGAGGGGTGGTTTCAGAGGAGGGTCAGGTGATGGGAAGGCAGGATGAGAAAAGCCCTGGACTTGCATGTTTGAGAAG
GCTTCCAACCACATCTTCACTCAGACTCTTGGAATTCCTGTCCCCAAAACAAGCTTCTGTTTTTTGCTCACAATGCTATATTTCTAAATT
TTTCCTGAATTACTGAGAAGCAGTCATTAGCTTTGTTAAGTTTGGTTTGGGGACATTGTTGGTATCAAAAATCGAAGTCTTATTCATTTG
ATGTAGGCCATGAATCATCAATAACTGGTTGCTGGAAAGCTTGACTACCATCCACTGGGGTGCTATTTTGAGAAGGATTTTTGGGTATCT
TTATAGTCTGCAATTAGTTGATGATTGCTTTCTAGTTTATCAACTGCATTTATATTTGCTTTTCTGTTCATGGAAAATCCTTTATTTGCT
GGGGTTTTTTGTTTGTTTGTTTGTTTTTCCCACTTACAGCAAGTAAAAGTGGTCTGAGGTTATCCTTGTTTTTCTTCGCGGTTTGCCATG
TGTGAAAGTAGATTTCCTGCTATTGATATATTCTCATTATAGACAGAATAGTGGAGAACAGTGTTGCCATGGACAAAATCCAGTTTTGGT
CCACTCTGGGGAGCATTTGGACCTGTGGTGCTTCTAACAATTAAAAGTCTAGATGGTCCTTGACTGTCCCCCAGCCATACTGCATACTAC
TTTGTGCATTCTACTTTGTGTCATTAATGAAAGATTGGTTCTGTCCCTGTAACTTAGGCATTTATTATTCTTAACTCTTCATTCCTGTTC
TGTAGCCACCCAGCAGTCCATTTTCCCTATGTTCAGGCCAAACCACAGGGCATTGGGGAAGGTTTTTGGGATTTTCTTATTGAGATTTTG
TTGAATCTGTAGTTTACCCCAGCTTTCCTAAGGTACAGTGAGGGGTTGGAGGGATCTGTGTTTGGCCCGGGGAGCAATTGTCTCTACCTT
AAGGTTCAGTTTTGAGGGCATAAAATACTACTTTGCAATGTCATGAGAACACCGTTAGATCTGAAATGTGGAAATGGTTTCTCACAATTT
AAAGGAAAAACCCACTTTGCACCCATGATCCCATCATTTTGGTTGAGATTTTAGAATAAAAAATATAGTGTTGAGATCCGTACTTTTGTA
ATCAGACCACCAAGCATGCCTGTGGCAAGGCAGAGAGGAAAGGTCTGGAGCCAGTGTATTGCAGTTTCATGCTACCTTTACCTGCTAATC
ATAAAAATTATGTTTTCAAAAGTAGATGATACTAGCCTTACACCCAAAAACATGTTCTGAATTAGATGCCCCCTCACCCAATTTTTATTA
AGCTTTCTAAATTCCAGCCACATTGCTGTACATCAACATTGGTTTCATTCAACAGACATTTTTTTGGCCTGAAGATACAAGGTTCAGAAA
GAGGCCATCCCTGCCCTCAAATAACTTTCATACTGGTGTATGATGAACTGACCATTAATAGTTTAAGTGCTTACAAGCTATGTTTCTGTT
CAAAAAAAAAATAGTTTGGTATAATAAATGCTATAAACCAATACACATTTCTGACTTGGGGGCAGAGACAGACTGGCTGATGTTGTATAG
TTTGTAGCCCTGGAGTAAGAAGTTGACATTAATTTCGGCCTATATGTGGAAAAGACCTATAACATTGGGTGAACTGAGCCAGCTGGCCAT
AGAACACAAGAACATATTCCAGGAAATAAATATAGCTGGAGGGTTGGAAATGCTGTTATTACTGAGAGAGAAAACAGGTGAGTTGGGATT
GAGAACTCCTGATTTTCATCCCTGGTTTAGATTCTTGGCCAAAGTAGTGGTAGAGTTAATCTTTGCTTGTGGAAAGCATTAACTATGTTG
CAGATTCAGTTGTGTTACATTATTGTGGGTTCTATAACAACATATTCCTCATGGACACTTTACCAGAGTTGCTCACACCTTTTTCAATTT
CTCATCCCTTTTGGAGGAATGAACATGAGACTTAACTGCCTTTAAGCCTAAAACGGACATGCTTTCCAATGACAAGAGATTTTCTAAAGA
GAAGTCTTGGAGCACATCTGTTAATACCTGAGCATCTACTCTGAGCAGTGCAGTTTTATTCAATACTGGAGAGAGGGTGATTTCTTTTTT
TTTGAGACGGAGTCTTGCTCTGTCTCCCAGGCTGGAGTGCAGTGGCGCAATCTCGGCTCACTGCAAGCTCCACCTCCCGGGTTCACGCCA
TTCTCCTGCCTCAGCCTCCCGAGGAGCTGGGACTACAGGCGCCGGCCACCACGCCCGGCTAATTTTTTGTATTTTTAGTAGAGACGGGGT
TTCACCTTGTTAGCCAGGATGGTCTCAATCTCCTGACCTCATGATCCACCCACCTCGGCCTCCCAGAGTGCTGGGATTACAGGCGTGAGC
CACCGCCGGGCCGAGAGGGTGATTTCTAAGCAGAGAATTGTATCAGTTATGTGGAAACCTTTGCCAGAAATACATATACCTTGTATATTA
AATCTGAGTCTCAGATTTAATCATCGAAGCGTAGCTGGGTTAAGAAACAGTCTGATCGTAAGGATGTTGTCGATTCTGACCCATGGATGA
CCACAAGAAAAAGATATTTATTTCTGCCTGGATAATTGAGAGTTGACTAACTTTGGAAGTCAGAATTCCCAGGAATTAGAGTAACTGCTC
TGGAAAGTTAAAGTGTGAAGTTTTTTAGATAGTTTCATAAAAACAATTCTGGTTTCTTTTTGCTTGTGCTGACTTTCTTGGATTTTAATC
TACCTCATCTTGTCTTTTTAGAGTTACTTCAACTTGTCACTTTAACATTGTGCTTGACTTTGGTTGTTTTCTAAGATGGAATTTTTCCTG
TTCATTGACAGCTTGTTCTCTTGCCTTTTCATTCTGATCCTCATTTCATCTAACATCATCTCATATTGCTCCTCTGTCAAGAGAAATGTT
TTAAAATAGTTTAAAGTCTTGTTTTATGGGAAGAAAGTGATCCTCCAATGCTATTTGTTTCTGAGGTCAGTAAGAGAAGGAGTTAAAACA
AGGCAGTGGGGAAGGGAATGAATCCTGCACTGGAGGCAAAAGCTGACAAGGAAAGAGCCATTAATTAAGACAATTTCAAAGTCAACTGAT
TGTGATCATTAATGTCACAATAGATCAAAACCTAATTATCACAGCCTAGGTAAGAGCCATCAGTATTAATCGGAAAATCTAATAGGAAAC
TATTATCAAGAAATTAGGCCAAATTGAATGCAGTGAACTTTTTATCTTGGCATTCTCTATTTTTTTGTGATGTCCCCTGGCATTGGCAGG
TGTGACCCTAACAGTCGATTCAAGGCCAAGTGGTCAGTTTGTCAGCCTTTTTTAAGGGATTTCTTTTTATTTTTAGGAATTCCAAACAGA
GTTAACCTAAACTGTCATTGCCAAAAGATCAGTCTTAAACTTTCTTAGCACCTGTACCTGTTTAATGTGATCAGCTATCAGTGAGGAAAA
AAAAAAAAATCTATTTAGGTCTTGGAATGGTTCCTGTACCTAGAGTATCCATATTGAACCTTTTTTTTTTTTTTTTTTTTTTTTTTTTGA
GATGGAAACTTGCTCTTTTGCCCAGGCTGGAGTGCAGTGGCGTGATCTTGGCTCACTGCAACCTCCGCCTCCCGGGTTCAAGCAGTTCTC
TGCCTCAGCCTCCTGAGCAGCTGGGATTATAGGCGCCTGCCACCATGCCCGGCTAATTTTTGTATTTTTAGTAGAGACAGGGTTCACCAT
CTTGGCCGTGCTGGTCTTGAACTCCTGACCTTGTGATCCGCCTGCCTCGGCCACTCAAAGTGCTGGGATTGCAGGCGTGAGCCAGCACCC
GGCCACAGTATCTTTATTACAGCTCACTGCAGCCTCAATCTCCTGGGCTCAAATGATCCTCCTGCCTCAGCCTCCCAAGCAGCTGGGACT
ACAGGCGCACACCACGGTGTCTGGCTAATTTTATTATTTAAAAAATGTTTTGTAGAGACAGTCTCCCTGTGTTGCCCAGGCTGGTCTCCA
ACTCGTGAGCTCAAGTGATCCACGTGCCTCAGCCTCCCAAAGTGCTGGGATTACAAGCATAAGCCACCGCACCCGGCCCCTAGTGAACAT
TTTACTGTATGTGTTGATAAATCATCTTTTGAGTTTCTGTTGTATGTGGGGACTTCCTACACTGGCTGCTGTGAAGAGGTATGGAAGAAA
GGAGAGGCTTTCTGCCTAGAAATTCTTTGAGAACACCTGAAAAGACAGTTTAATCATGTCACAACACTCTTAAGGCTCAAGTCAGTGTTC
TGGTTTCCGGTAGCTTTAGGATTGGATTCTAAACGAGGGCTGGTGGTGAGTTTGGTGTTTGTCTCGTGTCACCCTCACCCCTCACCTCCT
CAGTTTAGGATAAGAGACATAATGATTTCTACCAGAATCCAAAGTAAATCCAAAGGGGGAGAAAAGACATAACTGTTTTTTCTTCTACCT
TTTTTTTGTTAAAGAGTTACATCTCTCACAGGAGGAAAGAATTCAAGAGTCTATATGATTAGTTACAGAGAATATTTTCATCCCCTCTCC
CTGAATAGAAAAGCAGGGGTCACCATTTGTATCCTTACCCTTGAGGTGTTTTTGAAGATGCTGTAACTCTTGAAGTTGAGCTGAGGCAGA
AAGGTTGGAAAAATGCAGCCCTCTGGGTATTGTGGGGAGGGATGTGATGTAGTAAGAGGGTGTTTTGTGGTGCTAGGATTCCCACGCCAC
CAACTTGCAGCTTTATAAGAGCGCTACCAAGAACCACCACTGGGGAAAAGGTTCTTATTCATTGTTTCTGTTGGAATGTGATCTTGCTTT
CTGGATTTTAGGAATTCAGGTTACTCAGTATAAAACTCTGAGAAATCAGTGTGACTTAGTCCTTCACCTCCTAAGATAAAGTGAATATTT
CTTTACAAAATAATTCATGTCCTTAATGTTAAAGATGTAATTTTATTTTCAAAACATCTATAACATGACTTTCAGAAGCAGTTCATTTTT
CCAAGATTCCTCACATTATACTAGATAAATAATAGGCCCTCAGTTAATACCCTTCAGTTATTGAATTAATCTAGTTTGTGGAATGAGGTG
TATCCTGCCAACTTCCCTCTGCTCCCAAGTACACTCTGAGAGGTAAAATGCTCTGGGAAATGGAACAAGAATCGAGTGGATGCTGACTCT
GTGTGCCCACCTCCTCAACTGATTGATAATGGTTGACCTTGGGCAAGTCACTTCTTTCAATGCCTCAGTTCCCCATCTGTCAAATGGGGT
TAATAATACTGACCTACCTCACAGGGGTGTTGTTGTGAGGCATTGTAAATCAAAGTTAATAGAATACTTCAGGGTCCTCTGTGGAGGATG
TCTTGAGCCAGAGTTTAAGCCTGACACACAGGCTTTGGTCCTCACTGAGCTGTCTCCAAGACTGGAACTACTTAGTGACTCGGCAAATTT
TCTGCCCCCCACCCCTCATCAAAGCTGCTAGTTCAGATGTTGACAGTGTTTTCATGAATGTTGGAATCTTACTAGTCCAGACTTACTTAG
GATGTTGTTGGGGAAGGCACTTGGGATTTTCTGTGTCTTGCATTCACAGAGGGAGGCCATTTCAGATTCAAGAGCATTGGATTAGGGAAT
CGTGAGGCAGGGATGCTACTGCGTATTTCTCTCTGCAGGTTGGGGATTAAAGTTCCTTTCCCCATGGGTTTGAAGCAGACTCAGACTGTC
TCAGGATCAAAGCAACCCTCAATGGTTTTGATTTATGTCATTGCTTACCACTCCCCAACCAATCCCAGGACAGCTGGGTCACTGTACCCC
TTTGTGGTATCTGTACCTGGGCCTCTCCTTCCTCATAGGGACCAGCTGATTGAATAAATGTGACCACCTTATTTCCACCCCCCACCCCCA
AAAGCTACATTGGAATTATTTTTCCTAGAAATGTGTATAACACTCAGAATTGGGCATTGATCCTTAAAGCTTCATCCCATTCACCGTATT
CAACATCTGTCATCTCTTAGTGTCTGCAGTCTGAACCTAACCTTGACCTTTTTTCCCTCTGGTTTGAGAAAACTTTGGACACTATTTCTA
CTTGGCCAGGTGTGGGCTCAAGAGCCTTACTCTTTCCATCTCAGTTTAGGGGCGCAGCCAGCTCCTCTTCCCAATAGGGCTCTTTCTGCT
TTCCCTCTCCTTGGCCCTAGATTTGTAATCCATGAAAAAGCACAAGGTCCTGGCTCCTTGCGGTCACATTCTGGTTCTCTGTGTTTTGTG
GACTCTGCTCTCACTGTTCACCCAGCACTAGCAGTACCAGATGGTTCTGTGGAGTCCTGGGGAATGGAGAGAGCACAGTCTGACTCCCTG
CCAAGTAGCCAGGAGTTGACTTGCCCATGGTCCGCTGGCTTTCCCACCACTTCCTACAGGATGGGATCTAAGAGACTCAAGAGCTGGGTT
TCTTTCAGCACTCTGTACTGTCCCAAATAGCAAACAAATCACTTTGTAGCCAGATTTCTGAATGGAAATGAGAAATTGAATTCTCCATGG
ACTTTTAGGTTTATGGGGGAGTTTTAGCTGTGTTTCTTGGTTTTATTTCAGCCAAACATGTCTGCTTTTGATTTTTTTTTTAAAGTATAA
GTGGTCTATATATATGTTCACCTTTTAAATGTAAATGTTTAAAAAGTAAGCATTTATGTGTTTCCATAACTGACATCTGATGCAGACCTC

>7995_7995_1_ATP5I-CBX5_ATP5I_chr4_667092_ENST00000304312_CBX5_chr12_54635689_ENST00000209875_length(amino acids)=157AA_BP=
MSSLSVCSLNLTLTFFPSGLRKLWTLFLLGQVWAQEPYSFHLSLGAQPAPLPNRALSAFPLLGPRFVIHEKAQGPGSLRSHSGSLCFVDS

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Fusion Gene PPI Analysis for ATP5I-CBX5


check button Go to ChiPPI (Chimeric Protein-Protein interactions) to see the chimeric PPI interaction in

ChiPPI page.


check button Protein-protein interactors with each fusion partner protein in wild-type (BIOGRID-3.4.160)
HgeneHgene's interactorsTgeneTgene's interactors


check button - Retained PPIs in in-frame fusion.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenStill interaction with


check button - Lost PPIs in in-frame fusion.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenInteraction lost with


check button - Retained PPIs, but lost function due to frame-shift fusion.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenInteraction lost with


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Related Drugs for ATP5I-CBX5


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.8 2021-05-08)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status

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Related Diseases for ATP5I-CBX5


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
TgeneC0009402Colorectal Carcinoma1CTD_human
TgeneC0009404Colorectal Neoplasms1CTD_human